Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BrightView model number: 882478 BrightView X model number: 882480 BrightView Recalled by Philips Medical Systems (Cleveland) Inc Due to Unintended detector and gantry movement due to software...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips Medical Systems (Cleveland) Inc directly.
Affected Products
BrightView model number: 882478 BrightView X model number: 882480 BrightView XCT model number: 882482 and 882454 Medical Device for imaging
Quantity: 1064 units
Why Was This Recalled?
Unintended detector and gantry movement due to software issues.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Medical Systems (Cleveland) Inc
Philips Medical Systems (Cleveland) Inc has 313 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report